4.5 Article

Singlet Fission in Thin Solid Films of Bis(thienyl)diketopyrrolopyrroles

Journal

CHEMPLUSCHEM
Volume 85, Issue 12, Pages 2689-2703

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/cplu.202000623

Keywords

optical spectroscopy; photophysics; singlet fission; thin films; triplet excitons

Funding

  1. Ministry of Education, Youth and Sports of the Czech Republic - Program INTER-EXCELLENCE [LTAUSA19066]
  2. Grant Agency of the Czech Republic [19-22783S, 19-22806S]
  3. Institute of Organic Chemistry and Biochemistry [RVO: 61388963]
  4. U.S. Department of Energy, Office of Basic Energy Sciences, Division of Chemical Sciences, Biosciences,and Geosciences [DE-SC0007004]
  5. project e-Infrastruktura CZ [e-INFRA LM2018140]

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The singlet fission (SF) process discovered in bis(thienyl)diketopyrrolopyrroles (TDPPs) can boost their potential for photovoltaics (PV). The crystal structures of TDPP analogs carrying n-hexyl, n-butyl, or 2-(adamant-1-yl)ethyl substituents are similar, but contain increasingly slipped stacked neighbor molecules. The observed SF rate constants, k(SF), (7 +/- 4), (9 +/- 3) and (5.6 +/- 1.9) ns(-1) for thin films of the three compounds, respectively, are roughly equal, but the triplet quantum yields vary strongly: (120 +/- 40), (160 +/- 40) and (70 +/- 16), respectively. The recent molecular pair model reproduces the near equality of all three k(SF) at the crystal geometries and identifies all possible pair arrangements in which SF is predicted to be faster, by up to two orders of magnitude. However, it is also clear that the presently non-existent ability to predict the rates of processes competing with SF is pivotal for providing a guide for efforts to optimize the materials for PV.

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